Download Antifilarial Lead Molecules Isolated from Trachyspermum ammi

Molecules 2008, 13, 2156-2168; DOI: 10.3390/molecules13092156
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molecules
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Article
Antifilarial Lead Molecules Isolated from Trachyspermum ammi
Nisha Mathew 1,*, Shailja Misra-Bhattacharya 2, Vanamail Perumal 1 and
Kalyanasundaram Muthuswamy 1
1
2
Vector Control Research Centre (ICMR), Indira Nagar, Pondicherry-605006, India. E-mails:
[email protected] (V. P.), [email protected] (K. M.)
Division of Parasitology, Central Drug Research Institute, Lucknow 226001, India. E-mail:
[email protected] (S. M-B.)
* Author to whom correspondence should be addressed; E-mail: [email protected];
Tel.: 91-413-2272396; Fax: 91-413-2272041.
Received: 8 August; in revised form: 1 September 2008 / Accepted: 3 September 2008 / Published: 11
September 2008
Abstract: Lymphatic filariasis is caused by infection with the parasitic filarial nematodes
Wuchereria bancrofti, Brugia malayi and B. timori, transmitted by mosquitoes. The lack of
an adulticidal drug poses a challenge to filariasis elimination, hence it is essential to
develop an effective antifilarial drug which could either kill or permanently sterilize the
adult worms. In the reported work the in vitro activity of a methanolic extract of fruits of
Trachyspermum ammi (Apiaceae) against adult bovine filarial Setaria digitata worms has
been investigated. A bioassay-guided fractionation was carried out by subjecting the crude
extract to flash chromatography. HPLC analysis was done for the crude extract and active
fraction. The crude extract and the active fraction showed significant activity against the
adult S. digitata by both a worm motility and MTT [3-(4,5-dimethylthiazol-2-yl)-2,5diphenyltetrazolium bromide] reduction assays. The isolated active principle was
chemically characterized by IR, 1H-NMR and MS analysis and identified as a phenolic
monoterpene. It was screened for in vivo antifilarial activity against the human filarial
worm B. malayi in Mastomys coucha, showing macrofilaricidal activity and female worm
sterility in vivo against B. malayi. The findings thus provide a new lead for development of
a macrofilaricidal drug from natural products.
Keywords: Antifilarial; Thymol; Brugia malayi; Setaria digitata; Trachyspermum ammi
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Introduction
Lymphatic filariasis is caused by the infection with parasitic filarial nematodes Wuchereria
bancrofti, Brugia malayi and B. timori, transmitted by mosquito vectors. The drugs currently used for
lymphatic filariasis include annual doses of the microfilaricidal drug DEC (diethylcarbamazine), DEC
plus albendazole, ivermectin plus albendazole or the use of DEC fortified salt [1]. None of these is
effective in killing the adult worms, which can live in the host for several years [2] and the treatments
are therefore aimed solely at reducing transmission and pathology. Despite the important addition to
our knowledge of newer molecules [3-6] with antifilarial activity, none has developed fruitfully as a
macrofilaricidal drug due to their low antifilarial activity and/or high toxicity. This warrants the need
for developing an effective and safe drug to kill or permanently sterilize the adult worms. One of the
methods for identifying leads for drug development is to screen medicinal plants for the required
activity. Trachyspermum ammi (Ajwain caroway, family Apiaceae) is known for its antiviral [7], antiinflammatory [8], antifungal [9-13], molluscicidal [14-16], antihelminthic (in sheep) [17], plant
nematicidal [18], antipyretic [19], antiaggregatory [20] and antimicrobial activity [21-22]. This study
reports the antifilarial potential of the fruit extract of T. ammi against the adult bovine filarial worm
Setaria digitata. A compound obtained from T. ammi was identified and purified by bioassay-guided
chemical fractionation and screened for antifilarial activity against B. malayi in an animal model.
Results and Discussion
Plant extraction, purification and characterization
The yields of the crude residue after removal of the solvent from the T.ammi extract and the active
fraction after silica gel column chromatography (SGCC) were 14.15% w/w and 5.76% w/w
respectively. The residue of the crude extract was brownish coloured oily liquid. On repeated
chromatographic purification the active fraction yielded a white crystalline solid that by combined FTIR, NMR and mass spectral analysis was identified as 2-isopropyl-5-methyl phenol (thymol).
The comparative HPLC analysis of the crude extract, purified fractions and authentic 2-isopropyl-5methyl phenol (thymol) confirmed that the chromatogram of the active fraction matches that of
thymol, with a retention time of 6.04 minutes (Figure 1). Phenolic compounds of natural origin have
the desirable property of being soluble in polar solvents. This leads to the possibility of using reverse
phase HPLC (RP-HPLC) in their analysis. Sufficient retention time could be achieved by using acidic
conditions in order to avoid the presence of ionized forms of the analytes. The combination of RPHPLC and UV detection is widely used in both qualitative and quantitative analysis of Nature-derived
samples containing phenolics. The UV wavelength of 280 nm has proved to be suitable for universal
detection of all phenolics [23-24]. Here the thymol content was analyzed using Ultracarb C8 Column
using a mobile phase combination of methanol, water and acetic acid at 272 nm and a PDA detector.
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Figure 1. Overlayed HPLC analyses of T.ammi extract, active fraction and thymol.
T. ammi crude
T. ammi Fr 3
Absorbance (mAU)
Thymol
6.042
450
450
400
400
350
350
300
300
250
250
U
200
200
0.953
1.225
150
150
1.325
100
100
2.010
50
0.785
4.143
4.502
1.867
7.360
50
7.920
0
0
-50
0
2
4
6
8
10
-50
Time (minutes)
Antifilarial screening
The in vitro screening was carried out using adult S.digitata worms with the crude extract as well as
the fractions collected from the flash columns. Out of ten fractions collected, fractions 3-8 were pooled
based on TLC (Rf 0.68) carried out with precoated aluminium sheets with the hexane-ethyl acetate
(8:1) and these were found to contain the active principle. Other fractions were inactive. The in vitro
macrofilaricidal activity was assessed by worm motility and MTT reduction assay. Motility assay
showed complete inhibition of motility at higher test concentrations tested. Screening was carried out
at varying concentrations ranging from 0.001-1.0 mg/mL at two different incubation periods viz., 24
and 48 hrs to find out the dose response relationship as well as the effect of duration of exposure to the
test material on the viability of the filarial worms. The results of MTT reduction assay are given in
Table 1.
T. ammi crude extract exhibited macrofilaricidal activity which was quantitatively measured in
terms of percentage reduction in formazan formation with respect to the untreated control worms in
MTT reduction assay. The corresponding IC50 values were 0.067 and 0.019 mg/mL at two different
incubation periods 24 and 48 hr respectively. The IC50 values for the isolated active principle 2isopropyl-5-methyl phenol at two incubation periods 24 and 48 hr were 0.024 and 0.002 mg/mL,
respectively. The position isomer of the active principle 5-isopropyl-2-methyl phenol also showed
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macrofilaricidal activity with IC50 values of 0.025 and 0.004 mg/mL, respectively, for 24 and 48hr
incubation periods. The results showed a dose dependent effect on inhibition of formazan formation by
the test materials. It was also observed that at longer exposure period the compounds were more
effective showing that the compounds may be slow acting. The worm motility assay and MTT
reduction assay have confirmed the macrofilaricidal potential of the fruit extract of T. ammi and the
fraction obtained after chromatographic purification.
Table 1. In vitro macrofilaricidal activity of extract of T. ammi fruits against S. digitata
adult females by the MTT reduction assay, in comparison with the active principle and its
isomer.
S. No.
Test extract/
Compound
Incubation
period (hr)
1
T. ammi extract
24
48
2
2-isopropyl-5methyl phenol
24
48
3.
5-isopropyl-2methyl phenol
24
48
Test
concentration
(mg/mL)
% Formazan
formation
inhibition
± s.e (n=12)
0.01
0.05
0.10
0.50
0.005
0.01
0.05
0.10
0.50
0.005
0.01
0.05
0.10
0.50
0.001
0.005
0.01
0.05
0.10
0.005
0.01
0.05
0.10
0.50
0.005
0.01
0.05
0.10
11.88 + 1.57
30.84 + 1.49
53.59 + 0.96
92.30 + 0.78
21.26 + 0.82
36.74 + 1.04
65.12 + 0.48
80.96 + 1.21
93.43 + 0.75
20.77 + 0.93
34.29 + 1.16
60.80 + 1.87
76.94 + 0.47
97.61 + 0.61
35.43 + 0.93
59.35 + 1.41
71.64 + 0.84
85.39 + 0.45
94.18 + 0.19
24.25 + 0.75
31.08 + 2.49
54.00 + 1.15
76.47 + 0.77
95.61 + 0.17
25.88 + 1.30
68.82 + 1.31
80.44 + 0.54
95.83 + 0.46
IC50
(mg/mL)
All the compounds were screened at concentrations ranging from 0.001-1.0 mg/mL.
The concentrations showing <1% as well as >99% inhibition are not included in the table.
0.067
0.019
0.024
0.002
0.025
0.004
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The in vivo effect of the active principle 2-isopropyl-5-methyl phenol was evaluated against the B.
malayi parasite in a Mastomys coucha model. The observed adult worm mortality in treated and
control animals is shown in Figure 2. The mean percentage mortality of adults (58.93%) in the group
treated with 50 mg/Kg was significantly (Chi-square=56.2; P<0.0001) higher than that was obtained in
the control group (19.05%).
Figure 2. Adult worm mortality in treated and control animals.
% Adult worm mortality
90
80
70
60
50
40
30
20
10
0
1
2
3
4
5
6
7
Animal codes
Treated
Control
The percent sterilized (48.6%) in the group treated with 50 mg/Kg was significantly (Chisquare=11.54; P<0.0001) higher than that was obtained in the control group (17.8%, Table 2). The
results showed that the active principle isolated from T. ammi has promising in vivo antifilarial activity
in terms of adult worm mortality as well as female worm sterility. However the circulating
microfilariae were not affected by this compound at a dose level of 50 mg/kg, i.p. x 5days (Table 3).
Table 2. Sterilizing effect shown by 2-isopropyl-5-methylphenol in recovered adult worms
from treated Mastomys.
Group
Dose
(mg/Kg)
i.p x 5days
Number of
recovered females
teased
Number of
worms
sterilized (%)
95%
confidence
limits
Treated
Control
50
-
37
73
18 (48.6)
13 (17.8)
32.5-64.8
9.0-26.6
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Table 3. Effect of 2-isopropyl-5-methylphenol on B. malayi microfilaraemia density per 10
µL of tail blood in treated and control animals on pre- (0th day) and post-treatment days.
Days
Treated Group (50 mg/Kg.)
mean ± S.D
Control Group
mean ± S.D
0
29.1 + 13.6
54.3 + 18.8
8
45.7 + 12.0
56.4 + 12.6
15
61.4 + 19.4
61.4 + 18.9
30
73.4 + 23.6
65.9 + 19.6
45
78.0 + 24.9
75.0 + 25.3
60
86.9 + 29.8
84.4 + 20.3
75
109.0 + 31.7
103.9 + 32.8
90
119.6 + 33.6
108.3 + 33.1
Parasitic diseases are responsible for considerable morbidity and mortality throughout the world
especially in the tropical and subtropical regions. The morbidity caused by the important tropical
diseases,lymphatic filariasis and onchocerciasis, caused by infections with filarial nematodes, are
estimated at 951,000 DALYs (Disability-Adjusted Life Year- One DALY represents a lost year of
healthy life and is used to estimate the gap between the current health of a population and an ideal
situation where everyone in that population would live into old age in full health) for river blindness
and 5.5 million DALYs for lymphatic filariasis [25]. Present treatment regimens for these diseases
have limitations, as the currently used antifilarial drugs are mainly microfilaricidal, with little effect on
the adult worms and so new drugs are urgently required. In this regard, natural products have made
and continue to make important contributions to this therapeutic area. This study demonstrates that the
crude and purified extracts of T. ammi are effective in killing the adult bovine filarial worms in vitro.
The most important finding in this study is that the active principle has showed promising in vivo
macrofilaricidal activity as well as female worm sterility against human filarial worm B. malayi in M.
coucha.
Among the most promising advances in the field of drug development is discovering new molecules
or novel uses of the already available compounds with known safety and without any side effects.
Thymol is a naturally occurring phenolic monoterpene, known for its anti-oxidant and antiinflammatory potential in various disease conditions [26-27]. Use of thymol-containing preparations
for treating various diseases ranging from mouth washes and enteric disorders to skin infections is
common [22, 28-29]. The antimicrobial effect of (–)-menthol, thymol and linalyl acetate may be due,
at least partially, to a perturbation of the lipid fraction of bacterial plasma membranes, resulting in
alterations of membrane permeability and in leakage of intracellular materials [30]. Besides being
related to physicochemical characteristics of the drugs (such as lipophilicity and water solubility), this
effect appears to be dependent on the lipid composition and net surface charge of the bacterial
membranes. Furthermore, the drugs might cross the cell membranes, penetrating the interior of the cell
and interacting with intracellular sites critical for antibacterial activity.
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The essential oils of oregano (Origanum vulgare L.) and thyme (Thymus vulgaris L.) are effective
against Trypanosoma cruzi, with higher activity oberved for thyme, and thymol may be the main
component responsible for the trypanocidal activity [31]. Thymol showed considerable molluscicidal
effect against Biomphalaria alexandrina, Bulinus truncatus and Lymnneae natalensis [32]. Promising
antileishmanial and antimalarial potential has also been reported for thymol [33]. The main
constituent, carvacrol, but also its positional isomer, thymol, were tested. Interestingly, both
compounds retained the same activities observed for the oil. Furthermore, their trypanocidal activity
was even stronger (IC50 value for thymol: 114 ng/mL, for carvacrol: 149 ng/mL). Both the oil and its
two components are devoid of cytotoxicity on mammalian L6 cells (IC50 >50 µg/mL). Recently the in
vitro and in vivo antileishmanial and cytotoxic activities of thymol and structural derivatives were
compared to those of glucantime [34]. The reported results suggest that thymol and hemisynthetic
derivatives have promising antileishmanial potential and could be considered as new lead structures in
the search for novel antileishmanial drugs. None of the compounds seems to be toxic to the animals
based on corporal weight, behavior, and serum levels of bilirubin, uric acid, and glucose. While
complete cures did not occur, the absence of toxicity of these products will facilitate daily oral
treatment for longer periods.
Recently preliminary screening of T. ammi seed extracts for anthelmintic activity in sheep has been
reported [17], but the antifilarial potential of this important medicinal plant has not yet been exploited
fully. In the absence of an effective and safe antifilarial agent that could kill the long lived adult filarial
worm, it is worth exploring the possibility developing suitable pharmaceutical formulations for the
treatment of filariasis and the active principle could be considered as lead structure for development of
novel macrofilaricidal agents.
Conclusions
In summary, the methanolic extract of T. ammi has exhibited promising macrofilaricidal activity
against adult bovine filarial worm S. digitata and the active principle responsible for this has been
identified as thymol. The position isomer of thymol namely carvacrol also showed in vitro antifilarial
activity but to a lesser extent than thymol. The active molecule isolated from T. ammi has promising in
vivo antifilarial activity against human filarial worm B. malayi in terms of adult worm mortality as
well as female worm sterility.
Experimental
General
HPLC grade methanol, glacial acetic acid, analytical grade hexane, chloroform and absolute ethanol
(s. d. fine-chem., Mumbai, India), Dulbecco’s Modified Eagle’s Medium (DMEM) and foetal calf
serum (Sigma Chemical Co., St. Louis, USA), Strepto-penicillin (Sarabhai Chemicals, Baroda, India)
and MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) (Sisco Research
Laboratory, Mumbai, India) were used. Millipore filtered water was obtained by passing distilled
water through a Milli Q system (Millipore Corp., Milfed, MA). Dried T.ammi fruits were purchased
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locally, identified by a botanist and voucher specimen was kept for future studies. The FT-IR spectrum
was recorded on a Shimadzu FT-IR model 8300 (Shimadzu Corporation, Kyoto, Japan). 1H-NMR
Spectrum was taken on a GSX-400 (JEOL, Tokyo, Japan). Mass spectrum recorded on a GC-MS
(Finnigan Mat, Sanjose, CA). Spectrophotometric readings were taken in a SpectraMax Plus
(Molecular devices, Sunnyveil, CA) with SoftmaxPro software. HPLC system (ThermoFinnigan, CA)
composed of Spectra System P4000 solvent delivery system, Spectra System AS3000 autosampler and
Photodiode array (PDA) detector SN4000 was utilized. The output signals were monitored with
ChromQuest 4.0 Chromatography workstation.
Extraction, lead isolation and structure elucidation
Dried fruits of T. ammi (about 100 g) were powdered and used for each extraction with analytical
reagent grade methanol (500 mL) in a Soxhlet apparatus. After extraction, the solvent was flash
evaporated in a rotary vacuum evaporator for concentrating the extract (14.2% residue). A portion of
the residue was weighed and reconstituted in ethyl alcohol (30% w/v). This crude extract was screened
for macrofilaricidal activity after proper dilutions. Another portion was subjected to bioassay-guided
fractionation by flash chromatography. One gram of residue was subjected to SGCC with hexane-ethyl
acetate (8:1) as eluent on a 10 g FlashPack SIL connected to a Flashmaster Personal flash
chromatography system (Argonaut Technologies Ltd., Mid Glamorgan, UK). Ten fractions (10 mL
each) were collected. Fractions 3-5 and 6-8 were pooled based on TLC (Rf 0.68) carried out with
precoated (silica gel 60F254) aluminium sheets (Merck, Germany) with the hexane ethylacetate (8:1)
and solvent was removed to give a residue (0.407 g) which melted at 50-51oC. IR: 3442, 2961 and
1619 cm-1, characteristic of phenolic monoterpene; 1H-NMR: 1.21 (d, 6H), 2.23 (s, 3H), 3.2 (m, 1H),
4.3 (s. 1H), 6.5 (s, 1H), 6.76 (d, 1H), 7.1 (d, 1H). MS: 150 (M+), 135, 115, 101, 91, 71 and 57.
HPLC analysis of T. ammi extract
A simple and sensitive isocratic high performance liquid chromatographic (HPLC) method [35] was
used for the determination of active ingredient content in T. ammi extract. A 5 μm C8 reversed phase
Phenomenex Ultracarb analytical column (150 x 4.6 mm) and a mobile phase combination of
methanol-water-acetic acid (60:40:2) at the flow rate of 1.5 mL/min at 50oC were used for the analysis.
The residues from crude extract of T. ammi and the fractions obtained from SGCC were dissolved in
methanol and analyzed by HPLC using PDA detector seat at 272 nm.
In vitro screening for macrofilaricidal activity against S. digitata
Adults of the cattle filarial parasite of Setaria digitata (Nematoda: Filariodea), were used as the test
organism for screening the macrofilaricidal activity. Adult S. digitata worms collected from the
peritoneal cavity of freshly slaughtered cattle were washed with normal saline (0.85%) to free them of
any extraneous material and transferred to DMEM containing 0.01% Strepto-penicillin and
supplemented with 10% heat- inactivated foetal calf serum were used for the experiment within an
hour as reported earlier [36-37].
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Worm motility assay: Dilutions of the crude extract (30%w/v) of T. ammi were made in ethyl alcohol
and screening was done at concentrations ranging from 0.001-1.0 mg/mL. A simultaneous control was
kept with the vehicle ethyl alcohol alone in the medium. Two adult female S. digitata worms were
introduced into each Petri dish. Three replicates each were there for both test and control. The worms
were incubated at 37°C for 24 and 48 hrs in an incubator. After the incubation period the number of
immobilized worms in each petridish was counted. Immediately after counting, the worms were
washed twice with fresh medium and transferred to another set of Petri dishes containing fresh
medium, without the test solution, to find out whether any of the immotile worms regained motility. If
the worms did not revive, the condition was considered as irreversible and the concentration lethal.
Each experiment was repeated twice.
MTT- formazan colorimetric assay for viability of worms: T. ammi extract was further screened for
viability of adult S. digitata through a MTT reduction assay following the method reported earlier [38].
Adult female worms were used for this assay. After the exposure of the worms to various
concentrations of T. ammi (0.001- l.0 mg/mL) in DMEM at 24 and 48 hr incubation period, the
parasites were further incubated for 30 minutes individually in phosphate buffered saline (pH 7.4, 0.5
mL) containing MTT (0.25 mg/mL). A control was set up with adult females not treated with the test
solution but exposed to alcohol solvent as described in the above experiment. All the test
concentrations and controls were in 12 replicates. At the end of the MTT incubation, the worms were
transferred to a microtitre plate containing 400 µL of spectroscopic grade dimethyl sulphoxide
(DMSO) and allowed to be at room temperature for 1h, with occasional gentle shaking to extract the
colour developed. The absorbance of the resulting formazan solution was then determined at 492 nm in
a microplate spectrophotometer relative to DMSO blank. As the values of absorption correlate with
formazan formation, viability of the worms was estimated as percentage inhibition in formazan
formation relative to control worms. Similarly the pooled fractions obtained from flash
chromatography also were screened for macrofilaricidal activity. The antifilarial activity of the active
principle thymol (2-isopropyl-5-methyl phenol) was compared with the positional isomer of the active
compound carvacrol (5-isopropyl-2-methyl phenol).
In vivo screening for macrofilaricidal activity against B. malayi
The subperiodic strain of B. malayi was maintained in a rodent host, M. coucha, as reported
previously [39]. Male mastomys 6 weeks of age were infected by subcutaneous inoculation of 100
infective larvae (L3) of B. malayi recovered from mosquito vector Aedes aegypti on day 9±1 of
infected blood meal in the back region. M. coucha with a 5-6-month-old infection, showing a
progressive rise in microfilaraemia, were selected for in vivo evaluation. A total of 14 infected animals
were included in the study. Of these, seven animals were given the active compound at 50 mg/kg
intraperitoneally daily for five days while the other 7 animals served as controls.
The micro- and macrofilaricidal efficacy of the active fraction was evaluated as described earlier
[40]. A total of 10 μL of tail blood was taken from each animal and spread as a thick smear which was
air dried. The smears were dehaemoglobinized with water and later stained with Leishman’s stain. The
slides were viewed under a microscope at 10× magnification to assess the microfilarial density in the
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blood. Blood was taken on day 0 just before the start of treatment, and on days 8, 15, 30, 45, 60, 75
and until day 90 after treatment. Microfilaricidal efficacy in an individual animal was expressed as the
percent reduction in the density of microfilariae over the pretreatment level. A compound or fraction
was considered microfilaricidal on the basis of a fall in the microfilarial level on day 8 after the
treatment. Assessment of the macrofilaricidal/adulticidal efficacy of the extract was carried out by
evaluating the percent reduction in adult worm recovery in the treated group compared to untreated
animals. Treated and untreated animals were killed on day 90 after the start of treatment, and the heart,
lungs and testes were taken out and teased carefully to recover the adult parasites of both sexes. These
were examined for their motility, cell adherence on their surfaces, death or encapsulation. All
surviving females were teased individually in a drop of saline and the condition of the embryonic
stages in the uteri was examined microscopically. Any abnormality or death/distortion detected in the
uterine contents, including oocytes, eggs and microfilariae was considered as a sterilization effect of
the compound on the female [40].
Acknowledgements
Dr. Nisha Mathew expresses her sincere gratitude towards the International Foundation for Science
(IFS) and the Organization for Prohibition of Chemical Weapons (OPWC), Stockholm, Sweden for the
funding (Grant no. F/2929-1) to conduct part of this study. The authors are grateful to Dr. P. K. Das,
former Director, Vector Control Research Centre for his encouragement during the study. The
technical assistance rendered by Mrs. R. Anilakumari, Mr. S. Srinivasan is also gratefully
acknowledged.
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